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miRNA CT values from all TLDA plates were collected and CT distributions on each plate were inspected for data variability and sample anomalies.
Data from pH monitoring were visually inspected for data quality by MS and WS using the MMS International software tool (Medical Measurement Systems B.V., The Netherlands).
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Animals were inspected for ectoparasites (data not presented) before full necropsy was performed and body mass (minus gastrointestinal tract) recorded.
All of the predicted genes contained within the interval Os09g01690 (Os09g0104300)-Os09g38790 (Os09g0560900) were inspected for expression data, and there were nine genes with 4-fold changes, including a protein belonging to the Ulp1 protease family, an ethylene-responsive protein containing an AP2/ERF domain, an F-box-like protein, blight-associated protein p12, and a ribosomal protein.
Individual datasets were inspected for missing information, plausibility, and data entry errors.
Diffusion data were visually inspected for motion, including only data without visible motion.
Histograms of all variables were visually inspected for normality and the data were logarithmically transformed to compensate for the skewness of the data distribution.
Daily comprehension checks were collected and visually inspected for trends along with data on the number of challenging behaviors and social interactions displayed during intervention.
The best scored binding poses were manually inspected for compatibility with mutagenesis data reported for CCK derivatives binding to CCK-2R [27].
Each curve was visually inspected for artefacts, and such data were excluded.
Following initial linkage analyses, all markers not mapping to one of the expected 17 LGs were visually inspected for accuracy, to determine data quality, and to resolve any errors created by automatic allele calling in (Illumina).
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